FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GRASE BY DYNAMICS MS 27 SYRINGE DRIVER

K Number: K830809 · Decision Apr 14, 1983
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
211
Review Days
31

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Basic Information

Device Name
GRASE BY DYNAMICS MS 27 SYRINGE DRIVER
K Number
K830809
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Intermedics, Inc.
Date Received
March 14, 1983
Decision Date
April 14, 1983
Product Code
FRN
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRN Pump, Infusion

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Other Clearances by Intermedics, Inc.

K Number Device Name
K954610 MODEL 430-07 ENDOCARDIAL PACING LEAD
K955122 INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
K962174 BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)
K955550 CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD
K960281 IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY
K954719 INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
K933278 INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
K922042 CARDIFIX ENDOCARDIAL PACING LEAD
K922972 MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD
K920530 INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG
Search all 211 clearances from Intermedics, Inc. →